ISO 9001 vs. ISO 13485
What is ISO 9001?
ISO 9001 Certification means an organization has met the
requirements in ISO 9001. It defines an ISO 9000 Quality Management System
(QMS). ISO 9001 certification in Mumbai is focused on meeting customer expectations and delivering customer
satisfaction so you must pay attention to the customer.
In ISO 13485 Certification is the international standards
requirement for the quality management system for medical devices and related
services that consistently meet customer and applicable regulatory
requirements. In quality management system for special purposes the ISO 13485
Certification is standard for based on requirements of ISO 9001 Certification.ISO 13485 Certification services in New Zealand includes the entire ISO 9001
standard with additional requirements. One of the major distinctions of ISO
13485 is that it is intended to also be requirements for regulatory purposes as
well as non-statutory requirements for a quality management system.
What is ISO 13485
based on?
In ISO 13485 Certification is current version is released in
2003. In version is based on the version 9001 released in 2000 and it was
updated the ISO 9001 Certification in 2008. Most of the changes in ISO 9001 Certification in Lebanon were
clarification and added notes, with only a few minor updates that would affect
processes and procedures. In these changes is not necessary for medical devices
industry. So no updates to ISO 13485 Certification.
What are the
additional requirements in ISO 13485 Certification?
When it comes to the quality management system requirements
in sections four through eight, there are several small additions, mostly
involved in the identification and application of pertinent legal requirements
for the medical devices produced by the organization. Here is a brief listing
of the main additions:
Quality management
system:
·
In ISO Documentation requirements per
regulations.
·
Actions required maintaining effectiveness of
the QMS.
·
Records maintained for at least the lifetime of
the medical device or as specified by law.
·
Quality manual, to include scope of the QMS and
outline of documentation used.
Management Responsibility:
·
Responsibility & authority communication and
interaction of personnel to be ensured.
·
Management Rep to promote awareness of
regulatory requirements.
·
Management commitment to ensure effectiveness of
the Quality management system.
·
Quality policy, to include commitment to comply
with requirements and QMS effectiveness.
Product Realization:
·
Need for documented product requirements.
·
Purchasing procedures need to be documented.
·
In ISO 13485 Certification in Australia documented procedures needed for
monitoring and measurement.
Measurement, Analysis and Improvement:
·
In ISO measurement, analysis and improvement to include
quality management system effectiveness.
·
Feedback included in analysis of data.
·
Documented procedure required for a feedback
system to establish if the company has met customer requirements.
·
Including update of documents in the actions
taken for corrective actions.
·
Including records of investigations for
corrective and preventive actions.
By looking all reason everyone getting how the ISO 9001
certification will helps to employees in the your office. If you're looking to
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